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NCBI-Disease-Corpus-GPT5-withguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	217-254	DiseaseClass	denotes	disorder of fatty acid beta oxidation
T5	364-380	SpecificDisease	denotes	VLCAD deficiency
T6	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T7	460-472	SpecificDisease	denotes	hepatomegaly
T8	474-488	DiseaseClass	denotes	encephalopathy
T9	494-503	SpecificDisease	denotes	hypotonia
T10	535-551	SpecificDisease	denotes	VLCAD deficiency
T11	922-945	SpecificDisease	denotes	ventricular hypertrophy
T12	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T13	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-GPT5-noguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	12-18	Modifier	denotes	severe
T2	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T3	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T4	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T5	217-254	DiseaseClass	denotes	disorder of fatty acid beta oxidation
T6	364-380	SpecificDisease	denotes	VLCAD deficiency
T7	424-430	Modifier	denotes	severe
T8	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T9	460-472	SpecificDisease	denotes	hepatomegaly
T10	474-488	SpecificDisease	denotes	encephalopathy
T11	494-503	SpecificDisease	denotes	hypotonia
T12	535-551	SpecificDisease	denotes	VLCAD deficiency
T13	922-945	SpecificDisease	denotes	ventricular hypertrophy
T14	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T15	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	217-254	DiseaseClass	denotes	disorder of fatty acid beta oxidation
T5	364-380	SpecificDisease	denotes	VLCAD deficiency
T6	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T7	460-472	SpecificDisease	denotes	hepatomegaly
T8	474-488	DiseaseClass	denotes	encephalopathy
T9	494-503	SpecificDisease	denotes	hypotonia
T10	535-551	SpecificDisease	denotes	VLCAD deficiency
T11	922-945	SpecificDisease	denotes	ventricular hypertrophy
T12	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T13	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-Moderated1

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	217-254	DiseaseClass	denotes	disorder of fatty acid beta oxidation
T5	364-380	SpecificDisease	denotes	VLCAD deficiency
T6	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T7	474-488	DiseaseClass	denotes	encephalopathy
T8	535-551	SpecificDisease	denotes	VLCAD deficiency
T9	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T10	1149-1163	DiseaseClass	denotes	cardiomyopathy

sentences

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T1	0-146	Sentence	denotes	Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
TextSentencer_T2	147-313	Sentence	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency is a disorder of fatty acid beta oxidation that reportedly has high rates of morbidity and mortality.
TextSentencer_T3	314-504	Sentence	denotes	We describe the outcome of a 5-year-old girl with VLCAD deficiency who was first seen at 5 months of age with severe hypertrophic cardiomyopathy, hepatomegaly, encephalopathy, and hypotonia.
TextSentencer_T4	505-591	Sentence	denotes	Biochemical studies indicated VLCAD deficiency caused by a stable yet inactive enzyme.
TextSentencer_T5	592-723	Sentence	denotes	Molecular genetic analysis of her VLCAD gene revealed a T1372C (F458L) missense mutation and a 1668 ACAG 1669 splice site mutation.
TextSentencer_T6	724-917	Sentence	denotes	After initial treatment with intravenous glucose and carnitine, the patient has thrived on a low-fat diet supplemented with medium-chain triglyceride oil and carnitine and avoidance of fasting.
TextSentencer_T7	918-1036	Sentence	denotes	Her ventricular hypertrophy resolved significantly over 1 year, and cognitively, she is in the superior range for age.
TextSentencer_T8	1037-1176	Sentence	denotes	Clinical recognition of VLCAD deficiency is important because it is one of the few directly treatable causes of cardiomyopathy in children.
T1	0-146	Sentence	denotes	Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
T2	147-313	Sentence	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency is a disorder of fatty acid beta oxidation that reportedly has high rates of morbidity and mortality.
T3	314-504	Sentence	denotes	We describe the outcome of a 5-year-old girl with VLCAD deficiency who was first seen at 5 months of age with severe hypertrophic cardiomyopathy, hepatomegaly, encephalopathy, and hypotonia.
T4	505-591	Sentence	denotes	Biochemical studies indicated VLCAD deficiency caused by a stable yet inactive enzyme.
T5	592-723	Sentence	denotes	Molecular genetic analysis of her VLCAD gene revealed a T1372C (F458L) missense mutation and a 1668 ACAG 1669 splice site mutation.
T6	724-917	Sentence	denotes	After initial treatment with intravenous glucose and carnitine, the patient has thrived on a low-fat diet supplemented with medium-chain triglyceride oil and carnitine and avoidance of fasting.
T7	918-1036	Sentence	denotes	Her ventricular hypertrophy resolved significantly over 1 year, and cognitively, she is in the superior range for age.
T8	1037-1176	Sentence	denotes	Clinical recognition of VLCAD deficiency is important because it is one of the few directly treatable causes of cardiomyopathy in children.

PubCasesHPO

Id	Subject	Object	Predicate	Lexical cue
TI1	19-46	HP:0001639	denotes	hypertrophic cardiomyopathy
AB1	431-458	HP:0001639	denotes	hypertrophic cardiomyopathy
AB2	460-472	HP:0002240	denotes	hepatomegaly
AB3	474-488	HP:0001298	denotes	encephalopathy
AB4	922-945	HP:0001714	denotes	ventricular hypertrophy
AB5	1149-1163	HP:0001638	denotes	cardiomyopathy

PubCasesORDO

Id	Subject	Object	Predicate	Lexical cue
AB1	194-211	ORDO:26793	denotes	VLCAD) deficiency
AB2	364-380	ORDO:26793	denotes	VLCAD deficiency
AB3	535-551	ORDO:26793	denotes	VLCAD deficiency
AB4	1061-1077	ORDO:26793	denotes	VLCAD deficiency

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease:D002312	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease:C536353	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease:C536353	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease:C536353	denotes	VLCAD deficiency
T5	431-458	SpecificDisease:D002312	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease:D006529	denotes	hepatomegaly
T7	474-488	DiseaseClass:D001927	denotes	encephalopathy
T8	494-503	SpecificDisease:D009123	denotes	hypotonia
T9	535-551	SpecificDisease:C536353	denotes	VLCAD deficiency
T10	1061-1077	SpecificDisease:C536353	denotes	VLCAD deficiency
T11	1149-1163	DiseaseClass:D009202	denotes	cardiomyopathy

NCBI-Disease-Test

Id	Subject	Object	Predicate	Lexical cue	database_id
T430	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy	D002312
T431	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency	C536353
T432	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency	C536353
T433	364-380	SpecificDisease	denotes	VLCAD deficiency	C536353
T434	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy	D002312
T435	460-472	SpecificDisease	denotes	hepatomegaly	D006529
T436	474-488	DiseaseClass	denotes	encephalopathy	D001927
T437	494-503	SpecificDisease	denotes	hypotonia	D009123
T438	535-551	SpecificDisease	denotes	VLCAD deficiency	C536353
T439	1061-1077	SpecificDisease	denotes	VLCAD deficiency	C536353
T440	1149-1163	DiseaseClass	denotes	cardiomyopathy	D009202

NCBI-Disease-Test-Assistant-Knowledge

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	DiseaseClass	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	DiseaseClass	denotes	hypertrophic cardiomyopathy
T6	460-472	DiseaseClass	denotes	hepatomegaly
T7	474-488	DiseaseClass	denotes	encephalopathy
T8	494-503	DiseaseClass	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	922-945	DiseaseClass	denotes	ventricular hypertrophy
T11	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T12	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	12-18	Modifier	denotes	severe
T2	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T3	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T4	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T5	229-254	DiseaseClass	denotes	fatty acid beta oxidation
T6	364-380	SpecificDisease	denotes	VLCAD deficiency
T7	424-430	Modifier	denotes	severe
T8	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T9	460-472	SpecificDisease	denotes	hepatomegaly
T10	474-488	SpecificDisease	denotes	encephalopathy
T11	494-503	SpecificDisease	denotes	hypotonia
T12	535-551	SpecificDisease	denotes	VLCAD deficiency
T13	922-945	SpecificDisease	denotes	ventricular hypertrophy
T14	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T15	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	12-46	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	424-458	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T6	535-551	SpecificDisease	denotes	VLCAD deficiency
T7	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T8	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-high-o3-1

Id	Subject	Object	Predicate	Lexical cue
T1	12-46	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	424-458	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T6	535-551	SpecificDisease	denotes	VLCAD deficiency
T7	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T8	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-high-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-192	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase
T4	194-199	SpecificDisease	denotes	VLCAD
T5	201-211	SpecificDisease	denotes	deficiency
T6	364-380	SpecificDisease	denotes	VLCAD deficiency
T7	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T8	535-551	SpecificDisease	denotes	VLCAD deficiency
T9	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T10	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Test-4o-GuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	12-46	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	424-458	SpecificDisease	denotes	severe hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	922-945	SpecificDisease	denotes	ventricular hypertrophy
T11	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T12	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-UpdatedGuideline

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T11	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-humanintheloop

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	535-551	SpecificDisease	denotes	VLCAD deficiency
T7	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T8	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-rezarta1

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	DiseaseClass	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T11	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T430	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy	D002312
T431	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency	C536353
T432	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency	C536353
T433	364-380	SpecificDisease	denotes	VLCAD deficiency	C536353
T434	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy	D002312
T435	460-472	SpecificDisease	denotes	hepatomegaly	D006529
T436	474-488	DiseaseClass	denotes	encephalopathy	D001927
T437	494-503	SpecificDisease	denotes	hypotonia	D009123
T438	535-551	SpecificDisease	denotes	VLCAD deficiency	C536353
T439	1061-1077	SpecificDisease	denotes	VLCAD deficiency	C536353
T440	1149-1163	DiseaseClass	denotes	cardiomyopathy	D009202

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T11	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	DiseaseClass	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T11	1149-1163	DiseaseClass	denotes	cardiomyopathy

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	460-472	SpecificDisease	denotes	hepatomegaly
T7	474-488	SpecificDisease	denotes	encephalopathy
T8	494-503	SpecificDisease	denotes	hypotonia
T9	535-551	SpecificDisease	denotes	VLCAD deficiency
T10	777-786	SpecificDisease	denotes	carnitine
T11	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T12	1149-1163	SpecificDisease	denotes	cardiomyopathy

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	229-254	DiseaseClass	denotes	fatty acid beta oxidation
T5	364-380	SpecificDisease	denotes	VLCAD deficiency
T6	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T7	460-472	Modifier	denotes	hepatomegaly
T8	474-488	Modifier	denotes	encephalopathy
T9	494-503	Modifier	denotes	hypotonia
T10	535-551	SpecificDisease	denotes	VLCAD deficiency
T11	922-945	Modifier	denotes	ventricular hypertrophy
T12	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T13	1149-1163	DiseaseClass	denotes	cardiomyopathy

123456

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	SpecificDisease	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	535-551	SpecificDisease	denotes	VLCAD deficiency
T7	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T8	1149-1163	DiseaseClass	denotes	cardiomyopathy

12345

Id	Subject	Object	Predicate	Lexical cue
T1	19-46	SpecificDisease	denotes	hypertrophic cardiomyopathy
T2	89-145	SpecificDisease	denotes	very-long-chain acyl-coenzyme A dehydrogenase deficiency
T3	147-211	DiseaseClass	denotes	Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency
T4	364-380	SpecificDisease	denotes	VLCAD deficiency
T5	431-458	SpecificDisease	denotes	hypertrophic cardiomyopathy
T6	535-551	SpecificDisease	denotes	VLCAD deficiency
T7	1061-1077	SpecificDisease	denotes	VLCAD deficiency
T8	1149-1163	DiseaseClass	denotes	cardiomyopathy